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What is Statistical Power?

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University Course Reader · STEM

The trial had too little statistical power to detect a modest benefit, the authors cautioned, so its null result settles very little.

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Overview

Statistical power is the chance that a study will detect an effect that really exists, such as a drug lowering blood pressure by a few points. Four things set that chance before the study starts: how many people are measured (the sample size), how big the effect is, and how much the measurements vary from person to person. The fourth is how strict the cutoff is for declaring a result real. More people, a bigger effect, less variation and a looser cutoff all push the chance up. The rulebook for drug trials, the ICH E9 guideline, tells researchers to accept a 10% to 20% chance of missing a real effect. A trial that accepts 20% has 80% power: of five real effects, it finds four and misses one, by design. So a low-powered study that finds no effect has not shown there is none. The question to ask of any "no effect found" is how good its chances were.
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Overview

Statistical power is a study's odds of catching an effect that's genuinely there, like a sleep app that truly adds 20 minutes a night. Four dials control the odds, all set before day one: how many you test, how big the thing you're hunting is, and how much your readings wobble from one tester to the next. Dial four is how fussy your pass mark is for calling it real. Medicine trials run under a guideline, ICH E9, that lets them live with a 10% to 20% risk of missing a real effect. Live with 20% and you have 80% power, which sounds impressive until you count it out: hand that study five genuine effects and it waves one through as "nothing here", on purpose. That's why "study finds no link" is an opening line, not a verdict. The follow-up is how many they looked at and how big a link they could have spotted. A tiny study finding zilch is a shrug with a budget. 😎

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Detail

Statistical power is the probability that a study will find an effect that is really there. The effect is the difference being hunted: a drug lowering blood pressure by 5 points, say, against a dummy pill. Finding it means the result clears the cutoff for being called statistically significant, usually that chance alone would produce a difference this large less than 5% of the time. Missing a real effect is a false negative, and power is the chance of avoiding that miss. Four inputs set it. First, sample size: 400 patients give a better chance than 40, because the average of many is steadier. Second, effect size: a 5-point drop is easier to see than a 1-point drop. Third, variability: if blood pressure bounces around from patient to patient, a real 5 points hides in the scatter. Fourth, the cutoff: a stricter pass mark means more real effects fail it. The ICH E9 guideline for drug trials tells researchers to accept a 10% to 20% chance of a miss, so power of 80% to 90% (100 minus 20, 100 minus 10), and to recruit enough people to reach it. Why not 99%? Because finding an effect half the size takes roughly four times as many participants. A 2013 review estimated power across neuroscience studies at between about 8% and 31%, so most would miss a real effect more often than they found it. It also found a hidden cost: the effects such studies do find come out exaggerated, because only the readings that overshot by chance cleared the cutoff. So a null result needs a question put to it: what size of effect could this study have found? A found effect needs a different one: how big is it, which is effect size, not power. Power is whether a study can see the difference, not how much it matters.
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Detail

Statistical power is how likely a study is to catch a real effect, and it is decided before the first measurement. Take a fertiliser that genuinely adds 10% to a tomato crop. A trial can still report "no significant difference", and that is a false negative: the effect was there and the trial walked straight past it. Power is the trial's likelihood of not walking past. Four levers decide it. Lever one is how many plots: 200 beat 20, since averages calm down as you add more. Lever two is the size of the effect: a 10% boost is far simpler to spot than 2%. Lever three is noise: if yields swing wildly from plot to plot anyway, a genuine 10% drowns in the swings. Lever four is the bar: "significant" normally demands that luck by itself would manage it under once in twenty, and a fussier bar flunks more genuine effects. Medical trials work to a rulebook, ICH E9, that lets them accept a one-in-ten to one-in-five risk of a miss, which is 90% or 80% power. Nobody pays for near-certainty, because spotting a 5% boost instead of a 10% one calls for about quadruple the plots. A 2013 paper pegged the typical neuroscience study at 8 to 31 out of 100, so it walked past a genuine effect more than it caught it. The sting in the tail: when a weak study does score a hit, the hit is inflated, because only results that luck had pumped up cleared the bar. So treat "no effect found" as the start of a conversation: how big an effect could it even have caught? "Effect found" gets a second conversation, about how big, which is effect size, its own topic. Power is can-you-spot-it, not does-it-count. 😎

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Analogy

Statistical power is the chance a study finds an effect that is really there, and a search party for a lost dog works the same way. Three neighbours walk the woods for an hour and come back with nothing. Thirty people search until dark and come back with nothing. Only the second nothing tells you much about whether the dog is in those woods. Size matters too: three people would spot a Great Dane, while thirty might walk past a dachshund lying still in tall bracken. The searchers and their hours are the sample size, the dog's size is the effect size, the bracken and the failing light are the variability, and the rule for calling it found is the cutoff. A thin search that finds nothing tells you about the search, not the dog. The match ends here: a dog can wander off and an effect cannot, and the searchers eventually learn whether the dog was there, while a study never does.
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Analogy

Statistical power is a study's odds of noticing an effect that's really there, and noticing a friend's haircut is the same game. They took two centimetres off. You pass them in a corridor and clock zero. They shaved the lot off, and you'd spot it from across a car park. Sit opposite them through a whole dinner and even the trim registers, unless they keep a hat on all evening. How long you look is the sample size, two centimetres against a shaved head is the effect size, and the hat is the noise. How sure you want to be before you risk "did you get a haircut?" is the cutoff. "I didn't notice anything" after a corridor glance tells you about the glance, not the haircut. Where it stops matching: your friend can tell you the answer afterwards, and a study has no one to ask. 😎

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Formal definition β€” The same term, explained the usual way

Statistical power is the probability that a hypothesis test rejects the null hypothesis when a specified alternative is true: 1 βˆ’ Ξ², where Ξ² is the Type II (false negative) error rate. It is determined by the significance level (Ξ±), the sample size, the true effect size and the variance of the outcome, and is fixed at the design stage by an a priori power analysis that chooses the sample size for a minimum detectable effect. ICH E9, Statistical Principles for Clinical Trials (1998), Β§3.5: "The probability of type II error is conventionally set at 10% to 20%", i.e. power of 80% to 90%. Required sample size scales approximately with 1 Γ· (effect size)Β². Button et al., Nature Reviews Neuroscience 14, 365-376 (2013), estimated the median power of neuroscience studies at ∼8% to ∼31% and showed that low power also lowers the positive predictive value of significant findings and inflates published effect sizes (the winner's curse). Post hoc power computed from an observed effect is uninformative. Power concerns detection, not effect magnitude or importance.

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